Dispersion for 1-d Schrödinger and wave equations with bv coefficients

In this paper we analyze the dispersion for one dimensional wave and Schrödinger equations with BV coefficients. In the case of the wave equation we give a complete answer in terms of the variation of the logarithm of the coefficient showing that dispersion occurs if this variation is small enough but it may fail when the variation goes beyond a sharp threshold. For the Schrödinger equation we prove that the dispersion holds under the same smallness assumption on the variation of the coefficient. But, whether dispersion may fail for larger coefficients is unknown for the Schrödinger equation

First record of the alien leech Myzobdella lugubris leidy, 1851 (Hirudinea, Piscicolidae) in the Palearctic

In this study, we report the occurrence of the Nearctic leech Myzobdella lugubris in a brackish water body of the Riserva Naturale dello Stato “Le Cesine” (Apulia, Italy). Two specimens of the species were collected in October 2016 from the neck and the forelimbs of a European pond turtle, Emys orbicularis hellenica, and identified both based on morphology and molecular sequence data. In its native range, M. lugubris is known to be a host and vector of bacteria and viruses, among which some serious fish pathogens. In light of the possible noxious ecological effects exerted through pathogen spillover on autochthonous vertebrates, the distribution of the species and its possible role as a vector of pathogens in the invaded area should be urgently monitored

Influence Of Fusariosis In The Biochemical And Rheological Properties Of Different Wheat Cultivars

Fusarium spp. infection of cereal grain is a common problem, which can result in a decline of grain quality. The objective in this study was to understand the correlation between different degrees of infestation and the quantitative-qualitative changes in flour. The effects of different grades of infection of Fusarium were evaluated on: thousand kernel weight, wet gluten (WG), protein content, Zeleny sedimentation (ZS) and Falling Number (FN). Some of the most important rheological tests used in the industry were conducted on wheat flour of all varieties: Mixolab and GlutoPeak Test. The disease index average was 14.07 % varying from 4.07 % to 34.3% .The crude protein content was not significantly affected by the Fusarium spp. infection; on the contrary, FN, ZS and WG showed distinctively decreased values in all the infected cultivars

Alteration of the late endocytic pathway in Charcot–Marie–Tooth type 2B disease

The small GTPase RAB7A regulates late stages of the endocytic pathway and plays specific roles in neurons, controlling neurotrophins trafficking and signaling, neurite outgrowth and neuronal migration. Mutations in the RAB7A gene cause the autosomal dominant Charcot–Marie–Tooth type 2B (CMT2B) disease, an axonal peripheral neuropathy. As several neurodegenerative diseases are caused by alterations of endocytosis, we investigated whether CMT2B-causing mutations correlate with changes in this process. To this purpose, we studied the endocytic pathway in skin fibroblasts from healthy and CMT2B individuals. We found higher expression of late endocytic proteins in CMT2B cells compared to control cells, as well as higher activity of cathepsins and higher receptor degradation activity. Consistently, we observed an increased number of lysosomes, accompanied by higher lysosomal degradative activity in CMT2B cells. Furthermore, we found increased migration and increased RAC1 and MMP-2 activation in CMT2B compared to control cells. To validate these data, we obtained sensory neurons from patient and control iPS cells, to confirm increased lysosomal protein expression and lysosomal activity in CMT2B-derived neurons. Altogether, these results demonstrate that in CMT2B patient-derived cells, the endocytic degradative pathway is altered, suggesting that higher lysosomal activity contributes to neurodegeneration occurring in CMT2B

Reproductive biology of Diopatra neapolitana (Annelida, Onuphidae), an exploited natural resource in Ria de Aveiro (Northwestern Portugal)

Diopatra neapolitana Delle Chiaje, 1841 (Annelida, Onuphidae) is an important economic natural resource in Ria de Aveiro (northwestern coast of Portugal) and throughout Europe. The species is intensively harvested for use as fresh bait. However, there is only limited knowledge about its life cycle derived from a previous study in Mediterranean Sea. Reproduction and development patterns are known to vary biogeographically, making it important to base management decisions on locally appropriate information. This work examines reproduction patterns for populations from the Eastern Atlantic, which have not previously been assessed, with an eye towards drawing Atlantic–Mediterranean comparisons and informing local management strategies. The study was conducted from May 2007 to April 2009 in Ria de Aveiro. The reproductive biology of D. neapolitana was described from the proportional variation of worms with gametes in the coelom and from the progression of the oocyte diameter. Individuals with gametes inside the coelom were found all year round, but the peak reproductive period occurred between May and August, when almost all individuals had gametes in the coelom and females contained more oocytes than at any other time of the year. The overall male:female ratio was close to 1:1 and the oocyte diameter ranged from 40 to 240 μm. In vitro fertilization was performed and the results compared to other studies. Based on the present results, some protection measures are suggested to implement a sustainable exploitation of the species

p38-MK2 signaling axis regulates RNA metabolism after UV-light-induced DNA damage

UV-light-induced DNA damage affects RNA metabolism but the underlying signalling pathways are largely unexplored. Here, the authors show that UV light triggers p38-MK2-mediated phosphorylation of the NELF complex, promoting its release from chromatin and concurrent transcriptional elongation

Older Adults with Physical Frailty and Sarcopenia Show Increased Levels of Circulating Small Extracellular Vesicles with a Specific Mitochondrial Signature

Mitochondrial dysfunction and systemic inflammation are major factors in the development of sarcopenia, but the molecular determinants linking the two mechanisms are only partially understood. The study of extracellular vesicle (EV) trafficking may provide insights into this relationship. Circulating small EVs (sEVs) from serum of 11 older adults with physical frailty and sarcopenia (PF&S) and 10 controls were purified and characterized. Protein levels of three tetraspanins (CD9, CD63, and CD81) and selected mitochondrial markers, including adenosine triphosphate 5A (ATP5A), mitochondrial cytochrome C oxidase subunit I (MTCOI), nicotinamide adenine dinucleotide reduced form (NADH):ubiquinone oxidoreductase subunit B8 (NDUFB8), NADH:ubiquinone oxidoreductase subunit S3 (NDUFS3), succinate dehydrogenase complex iron sulfur subunit B (SDHB), and ubiquinol-cytochrome C reductase core protein 2 (UQCRC2) were quantified by Western immunoblotting. Participants with PF&S showed higher levels of circulating sEVs relative to controls. Protein levels of CD9 and CD63 were lower in the sEV fraction of PF&S older adults, while CD81 was unvaried between groups. In addition, circulating sEVs from PF&S participants had lower amounts of ATP5A, NDUFS3, and SDHB. No signal was detected for MTCOI, NDUFB8, or UQCRC2 in either participant group. Our findings indicate that, in spite of increased sEV secretion, lower amounts of mitochondrial components are discarded through EV in older adults with PF&S. In-depth analysis of EV trafficking might open new venues for biomarker discovery and treatment development for PF&S

Combined inhibition of Aurora-A and ATR kinase results in regression of MYCN-amplified neuroblastoma

Amplification of MYCN is the driving oncogene in a subset of high-risk neuroblastoma. The MYCN protein and the Aurora-A kinase form a complex during S phase that stabilizes MYCN. Here we show that MYCN activates Aurora-A on chromatin, which phosphorylates histone H3 at serine 10 in S phase, promotes the deposition of histone H3.3 and suppresses R-loop formation. Inhibition of Aurora-A induces transcription-replication conflicts and activates the Ataxia telangiectasia and Rad3 related (ATR) kinase, which limits double-strand break accumulation upon Aurora-A inhibition. Combined inhibition of Aurora-A and ATR induces rampant tumor-specific apoptosis and tumor regression in mouse models of neuroblastoma, leading to permanent eradication in a subset of mice. The therapeutic efficacy is due to both tumor cell-intrinsic and immune cell-mediated mechanisms. We propose that targeting the ability of Aurora-A to resolve transcription-replication conflicts is an effective therapy for MYCN-driven neuroblastoma (141 words)

Loss of Angiotensin-Converting Enzyme 2 Exacerbates Diabetic Retinopathy by Promoting Bone Marrow Dysfunction

Angiotensin-converting enzyme 2 (ACE2) is the primary enzyme of the vasoprotective axis of the renin angiotensin system (RAS). We tested the hypothesis that loss of ACE2 would exacerbate diabetic retinopathy by promoting bone marrow dysfunction. ACE2-/y were crossed with Akita mice, a model of type 1 diabetes. When comparing the bone marrow of the ACE2-/y-Akita mice to that of Akita mice, we observed a reduction of both short-term and long-term repopulating hematopoietic stem cells, a shift of hematopoiesis towards myelopoiesis, and an impairment of lineage-c-kit+ hematopoietic stem/progenitor cell (HS/PC) migration and proliferation. Migratory and proliferative dysfunction of these cells was corrected by exposure to angiotensin-1–7 (Ang-1–7), the protective peptide generated by ACE2. Over the duration of diabetes examined, ACE2 deficiency led to progressive reduction in electrical responses assessed by electroretinography and to increases in neural infarcts observed by fundus photography. Compared to Akita mice, ACE2-/y-Akita at 9-months of diabetes showed an increased number of acellular capillaries indicative of more severe diabetic retinopathy. In diabetic and control human subjects, CD34+ cells, a key bone marrow HS/PC population, were assessed for changes in mRNA levels for MAS, the receptor for Ang-1–7. Levels were highest in CD34+ cells from diabetics without retinopathy. Higher serum Ang-1–7 levels predicted protection from development of retinopathy in diabetics. Treatment with Ang-1–7 or alamandine restored the impaired migration function of CD34+ cells from subjects with retinopathy. These data support that activation of the protective RAS within HS/PCs may represent a therapeutic strategy for prevention of diabetic retinopathy